Clinical Research Coordinator I, Radiation Oncology - Remote

Overview

The Clinical Research Coordinator I will assist in clinical research studies, focusing on patient recruitment, data collection, and ensuring compliance with study protocols.

In Short

• Assist in recruiting and evaluating patients for clinical trials.
• Collect and organize patient data.
• Schedule patients for study visits.
• Perform clinical tests such as phlebotomy and EKGs.
• Maintain and update study data.
• Verify compliance with sponsor and organizational guidelines.
• Prepare data for analysis and entry.
• Document patient visits and procedures.
• Assist with regulatory submissions.
• Work collaboratively with a team of healthcare professionals.

Requirements

• Bachelor's Degree in a related field required.
• 0-1 year of relevant research project experience preferred.
• Attention to detail and strong organizational skills.
• Ability to follow directions and work collaboratively.
• Good interpersonal and communication skills.
• Computer literacy and knowledge of clinical research protocols.
• Respect for subjects' rights and individual needs.

Benefits

• Competitive base pay.
• Comprehensive benefits package.
• Career advancement opportunities.
• Recognition programs for contributions.
• Support for professional growth.